A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089443



Internal ID21998676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83183870..83183870hg38UCSC Ensembl
chr11:82894912..82894912hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597431
Samples
Known GenesPCF11
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089443
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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